exam 2 ch 13 Flashcards

1
Q

The branch of evolutionary biology that studies the diversity of reproductive
strategies

A

life-history analysis

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2
Q

Have a high growth rate but low survivability (“cheap” offspring)

A

r-selected species

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3
Q

Have a low growth rate but high survivability (“expensive” offspring)

A

K-selected species

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4
Q

Changes in life history are caused by changes in the?

A

allocation of energy

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5
Q

Number of gametes produced by an individual

A

Fecundity

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6
Q

selection will favor the number of offspring that results in the most surviving
offspring

A

Lack’s Hypothesis

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7
Q

individual offspring survival decreases with increasing offspring number

A

Trade-off

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8
Q

Energy contained in the offspring themselves

A

Direct costs

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9
Q

Energy expended to produce and carry them

A

indirect costs

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10
Q
  1. (a) There is a trade-off between size and number of offspring.
  2. (b) Above a minimum size, the probability that any individual offspring will survive is an increasing
    function of its size
A

Selection on Offspring Size
Assumptions

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11
Q

selection on Offspring Size

A

-Selection on parents favors a compromise
between the quality and quantity of offspring,
-Selection on individual offspring favors
high quality

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12
Q

Fertilization of two or more ova from the same cycle by sperm from separate
acts of sexual intercourse

A

Superfecundation

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13
Q

Only one copy of a gene in an individual (from mother or father) is expressed,
while the other copy is suppressed

A

Genomic imprinting

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14
Q

A growth promoting hormone.

A

Insulin-like growth factor II

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15
Q

A receptor that binds IGF-II to promote
lysosome activity

A

Cation-independent mannose-6-phosphate receptor (CI-MPR)

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16
Q

When mates are not monogamous, the life-history strategy that is ___________________________ for the other

A

optimal for one sex may be
suboptimal

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17
Q

Life-history traits have ________________________ than other traits.

A

lower heritabilities

18
Q

Low heritability means traits are more influenced by?

A

environmental factors

19
Q

Higher reproductive capacity allowed dinosaurs to?

A

recover more quickly from population bottlenecks

20
Q

Describes the molecular changes seen in most aging cells

A

The Hallmarks of Aging

21
Q

There are 2 main models of aging;

A
  1. Damaged-based model
  2. Programmatic models
22
Q
  1. Damaged-based model
A

(Damage to DNA and cells accumulates)

23
Q
  1. Programmatic models
A

(Aging is encoded in the DNA)

24
Q

Mammals with higher somatic mutation rates have ______ lifespans

25
non-sex cells
somatic cells
26
are highly reactive chemicals formed from diatomic oxygen (O2), water, and hydrogen peroxide. Some prominent ROS are hydroperoxide (-OOH), superoxide (O2-), hydroxyl radical (OH.)
Reactive oxygen species (ROS)
27
During DNA replication, at the end of the lagging the final RNA primer is removed leaving a small site that is not replicated by polymerase, meaning that there will be a small amount of DNA lost each time the cell divides.
End replication problem
28
A region of repetitive DNA sequences that protect the ends of chromosomes
Telomeres
29
As cells divide, the telomere ends of chromosomes get shorter
Telomere attrition
30
The limit on cell replication imposed by the shortening of telomeres with each division.
Hayflick limit
31
A reverse transcriptase that adds repeats of a DNA sequence to the ends of chromosomes.
Telomerase
32
There are 2 main models of aging?
1. Damaged-based model 2. Programmatic models
33
-Conserved methylation sites were highly enriched in polycomb repressive complex 2-binding locations, which represses the transcription of diverse developmental genes
Aging Clocks
34
Methylation clocks indicate aging has a predictable?
preset program
35
Age at which RNA expression pattern reverses direction
transcriptome Trajectory Turning Points (TTTP):
36
1. Damaged-based model
(Damage to DNA and cells accumulates)
37
2. Programmatic models
(Aging is encoded in the DNA)
38
Peak at ~age 26 =?
End of brain development = same time as onset of aging phenotypes
39
Adult cells reprogrammed back into an embryonic-like pluripotent state that enables them to become any type of cell.
induced Pluripotent Stem Cells (iPSC’s)
40
The transcription factors (Oct4 (Pou5f1), Sox2, Klf4 and cMyc) that were used to turn adult cells into Pluripotent stem cells
yamanaka Factors
41